Vitiligo-associated autoimmune disease

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 2
OrphanetNr: 247871
OMIM Id: 193200
606579
607836
608391
608392
609400
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset: Childhood
Adolescent
Adult
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Autoinflammatory syndrome with skin involvement
 -Rare skin disease
Mixed autoinflammatory and autoimmune syndrome
 -Rare systemic or rheumatologic disease

Symptom Information: Sort by abundance 

1
(HPO:0003764) Nevus 17 / 7739
2
(HPO:0001045) Vitiligo 13 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: